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Hereditary MTC syndromes include MEN2A, which is the most common, MEN2B, and hereditary non-MEN syndromes

It also marks this strategy as having high individual variability, tying the outcome to a person's baseline gut microbiota rather than to the fiber amount alone

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Transcriptome analysis of the mouse cellular models of Ube3a deficiency has revealed differential gene expression associated with mitochondrial pathways [381]

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